Canonical Allele Identifier: CA481317554
Gene: GNPTAB HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.102147191C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753413C>T , CM000674.2:g.101753413C>T GRCh38
NC_000012.11:g.102147191C>T , CM000674.1:g.102147191C>T GRCh37
NC_000012.10:g.100671322C>T NCBI36
NG_021243.1:g.82455G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3561G>A MANE Select ENSP00000299314.7:p.Glu1187=
ENST00000299314.11:c.3561G>A ENSP00000299314.7:p.Glu1187=
ENST00000549738.5:c.459G>A ENSP00000450161.1:n.459G>A
NM_024312.4:c.3561G>A NP_077288.2:p.Glu1187=
XM_011538731.1:c.3480G>A XP_011537033.1:p.Glu1160=
XM_011538731.2:c.3480G>A XP_011537033.1:p.Glu1160=
XM_017019961.1:c.3345G>A XP_016875450.1:p.Glu1115=
XM_017019962.2:c.2334G>A XP_016875451.1:p.Glu778=
NM_024312.5:c.3561G>A MANE Select NP_077288.2:p.Glu1187=